Plasminogen activator inhibitor 1 is an intracellular inhibitor of furin proprotein convertase

被引:37
作者
Bernot, Denis [1 ]
Stalin, Jimmy [1 ]
Stocker, Pierre [2 ]
Bonardo, Bernadette [1 ]
Scroyen, Ilse [1 ]
Alessi, Marie-Christine [1 ]
Peiretti, Franck [1 ]
机构
[1] Univ Aix Marseille 2, INSERM, Fac Med, U626, F-13385 Marseille 5, France
[2] Univ Paul Cezanne, Equipe Biosci iSm2 UMR 6263, FST St Jerome, F-13397 Marseille 20, France
关键词
ADAM17; Furin; Golgi; Insulin receptor; PAI-1; Convertase; NECROSIS-FACTOR-ALPHA; TRANSMEMBRANE TNF-ALPHA; INSULIN-RESISTANCE; ADIPOSE-TISSUE; ENDOTHELIAL-CELLS; SECRETORY PATHWAY; ENDOGENOUS FURIN; CUTTING EDGE; ENZYME; SERPIN;
D O I
10.1242/jcs.079889
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Proprotein convertases (PCs) are a family of serine proteases that are involved in the post-translational processing and activation of a wide range of regulatory proteins. The upstream role of PCs in the control of many physiological and pathological processes generates a growing interest in understanding their regulation. Here, we demonstrate that the serine protease inhibitor plasminogen activator inhibitor 1 (PAI-1) forms an SDS-stable complex with the PC furin, which leads to the inhibition of the intra-Golgi activity of furin. It is known that elevated PAI-1 plasma levels are correlated with the occurrence of the metabolic syndrome and type 2 diabetes, and we show that PAI-1 reduces the furin-dependent maturation and activity of the insulin receptor and ADAM17: two proteins involved in the onset of these metabolic disorders. In addition to demonstrating that PAI-1 is an intracellular inhibitor of furin, this study also provides arguments in favor of an active role for PAI-1 in the development of metabolic disorders.
引用
收藏
页码:1224 / 1230
页数:7
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